Caitlin Clohessy Email & Phone Number

• Run point on research project start-up, implementation, and all research activities through the lifecycle of over 50+ projects across 4+ clinical divisions. Collaborates with all project stakeholders to provide a.
• Provide direct supervision, professional development training, competency assessment and mentorship to a skilled team of research coordinators, whose responsibilities include the daily research activities of the.
• Oversee the collection, compilation, documentation, review, and quality assurance of clinical research data. Participates in routine audits safety evaluation, data quality analysis, regulatory compliance, and adherence.
• Support budget builds, regulatory submissions, contract agreements, and tracks deliverables and metrics, providing status reports to stakeholders
• As a multidisciplinary team leader, maintains ultimate responsibility for a variety of high-stakes research including investigational drug trials and gene therapy trials

Aurora, Colorado

• Managed daily operational needs of research trials while collaborating with financial analysts to anticipate budgetary issues and ensure project goals were being met financially and operationally
• Served as the lead liaison for Epilepsy and Headache trials in the Neurology portfolio for Sponsor-initiated FDA investigational drug trials as well as a formal mentor and resource for RI and hospital staff members..
• Collaborate with stakeholders and effective project from initial contract to close out
• Contributed to Research Institute process improvement as a leader for an SOP committee and RI Strategy focus group member

• Lead Coordinator for multiple industry and investigator-initiated research studies servicing patients across Colorado with primary responsibilities in defining and managing project resource needs, database management.
• Oversight of all trial-related activities via web-based database platforms, including IRB submissions, electronic database management as well as source document templating and revisions.
• Primary point of contact for all parties and liaison for primary study doctor, worked closely in tracking progress and identifying issues with contingency plans to achieve goals; completing on-time and on-budget.
• Conducted monitoring visits for quality assurance and compliance, relayed developments and progress to study team and sponsors.

Cincinnati OH

• Coordinated research and quality improvement studies on the Hospital Medicine service. Responsibilities included day-to-day research activities to ensure collection of high-quality data
• Responsible for research infrastructure and implementation support of studies, tracking logistical issues and creating relationships between various hospitals and departments for collaboration. Primary liaison between.
• Counseled and conducted qualitative interviews for study patients and their providers, analyzed and coded data collected, eventually
• Wrote, edited, and submitted copy for grant submissions to sponsors according to timeline. Authored and edited multiple medical manuscripts and figures prior to medical journal submission after completion of projects.

Bachelor Of Science (Bs), English Language And Literature

Education record